(R)-3, 3'-Bis[4-(1-naphthalenyl)phenyl]-1, 1'-binaphthyl-2, 2'-diyl Hydrogenphosphate

98%

Reagent Code: #231084
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CAS Number 1450925-06-0

science Other reagents with same CAS 1450925-06-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 752.79 g/mol
Formula C₅₂H₃₃O₄P
badge Registry Numbers
MDL Number MFCD30489111
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as a chiral Brønsted acid organocatalyst in asymmetric synthesis, enabling high enantioselectivity in reactions such as cyanosilylation, Mannich-type reactions, and other carbon-carbon bond formations. Its bulky, well-defined chiral structure derived from substituted BINOL provides effective steric and electronic control for stereoselective transformations, particularly in pharmaceutical and fine chemical manufacturing. Commonly applied in the synthesis of enantiopure compounds where precise stereochemistry is critical, without requiring transition metals.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,450.00
inventory 250mg
10-20 days ฿7,300.00
inventory 1g
10-20 days ฿25,600.00
(R)-3, 3'-Bis[4-(1-naphthalenyl)phenyl]-1, 1'-binaphthyl-2, 2'-diyl Hydrogenphosphate
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Used as a chiral Brønsted acid organocatalyst in asymmetric synthesis, enabling high enantioselectivity in reactions such as cyanosilylation, Mannich-type reactions, and other carbon-carbon bond formations. Its bulky, well-defined chiral structure derived from substituted BINOL provides effective steric and electronic control for stereoselective transformations, particularly in pharmaceutical and fine chemical manufacturing. Commonly applied in the synthesis of enantiopure compounds where precise stereoc

Used as a chiral Brønsted acid organocatalyst in asymmetric synthesis, enabling high enantioselectivity in reactions such as cyanosilylation, Mannich-type reactions, and other carbon-carbon bond formations. Its bulky, well-defined chiral structure derived from substituted BINOL provides effective steric and electronic control for stereoselective transformations, particularly in pharmaceutical and fine chemical manufacturing. Commonly applied in the synthesis of enantiopure compounds where precise stereochemistry is critical, without requiring transition metals.

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